• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[鼻咽癌中凋亡与增殖相关基因的筛查及初步分析]

[Screening and preliminary analysis of the apoptosis- and proliferation-related genes in nasopharyngeal carcinoma].

作者信息

Zhou Yi-bo, Huang Zhong-xi, Ren Cai-ping, Zhu Bin, Yao Kai-tai

机构信息

Cancer Research Institute of Central South University, Changsha 410078, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2009 Apr;29(4):645-7.

PMID:19403385
Abstract

UNLABELLED

To screen and analyze the apoptosis- and proliferation-related genes in human nasopharyngeal carcinoma (NPC).

METHODS

According to gene ontology classification, the abnormal expressions of the genes related to cell apoptosis and proliferation were identified in the NPC gene chip data. The cell apoptosis- and proliferation-related genes expressed in each of the 3 stages, as defined by the tree model for the pathogenesis and progression of NPC, were screened, and with literature review, their distribution in the tree model were analyzed.

RESULTS

Nineteen genes related to cell apoptosis were found in NPC, among which 9 were down-regulated (such as DNASE1L3) and located in the chromosome deletion regions, and 10 were up-regulated (such as DEDD) in the chromosome amplification regions. Twenty-one cell proliferation-related genes were identified, including 8 down-regulated genes (such as TUSC2) in the chromosome deletion regions and 13 up-regulated ones (such as EMP1) in the chromosome amplification regions. In the chromosome deletion regions, the down-regulated cell apoptosis-related genes participated mostly in inducing and regulating cell apoptosis, and the up-regulated cell proliferation-related genes in the chromosome amplification regions were mostly associated with the positive regulation of cell proliferation.

CONCLUSION

NPC occurs possibly through two pathways by inhibiting cell apoptosis or by promoting excessive cell proliferation.

摘要

未标注

筛选并分析人鼻咽癌(NPC)中与细胞凋亡和增殖相关的基因。

方法

根据基因本体分类,在NPC基因芯片数据中鉴定与细胞凋亡和增殖相关的基因的异常表达。筛选在NPC发病机制和进展的树状模型所定义的3个阶段中每个阶段表达的细胞凋亡和增殖相关基因,并通过文献综述分析它们在树状模型中的分布。

结果

在NPC中发现19个与细胞凋亡相关的基因,其中9个下调(如DNASE1L3)且位于染色体缺失区域,10个上调(如DEDD)于染色体扩增区域。鉴定出21个与细胞增殖相关的基因,包括8个下调基因(如TUSC2)位于染色体缺失区域和13个上调基因(如EMP1)于染色体扩增区域。在染色体缺失区域,下调的细胞凋亡相关基因主要参与诱导和调节细胞凋亡,而在染色体扩增区域上调的细胞增殖相关基因大多与细胞增殖的正调控相关。

结论

NPC可能通过抑制细胞凋亡或促进细胞过度增殖这两条途径发生。

相似文献

1
[Screening and preliminary analysis of the apoptosis- and proliferation-related genes in nasopharyngeal carcinoma].[鼻咽癌中凋亡与增殖相关基因的筛查及初步分析]
Nan Fang Yi Ke Da Xue Xue Bao. 2009 Apr;29(4):645-7.
2
[Gene expression profiling in nasopharyngeal carcinoma determined by high density cDNA microarray].[应用高密度cDNA微阵列技术检测鼻咽癌基因表达谱]
Ai Zheng. 2002 Jun;21(6):588-92.
3
[Differentially expressed transcription factor-related genes in nasopharyngeal carcinoma and nasopharyngeal tissues].[鼻咽癌与鼻咽组织中差异表达的转录因子相关基因]
Nan Fang Yi Ke Da Xue Xue Bao. 2007 Feb;27(2):146-9.
4
[Identification of differentially expressed genes in primary cultured nasopharyngeal carcinoma cells by cDNA microarray].[应用cDNA微阵列技术鉴定原代培养鼻咽癌细胞中的差异表达基因]
Nan Fang Yi Ke Da Xue Xue Bao. 2007 Aug;27(8):1156-60.
5
[Plerosis of cDNA array of normal human nasopharyngeal tissue and nasopharyngeal carcinoma].[正常人鼻咽组织与鼻咽癌cDNA阵列的修复]
Zhonghua Zhong Liu Za Zhi. 2002 Mar;24(2):114-7.
6
[Gene expression profiles in different tissues of human nasopharyngeal carcinoma].[人类鼻咽癌不同组织中的基因表达谱]
Di Yi Jun Yi Da Xue Xue Bao. 2004 Oct;24(10):1126-9.
7
[Differentially expressed gene in nasopharyngeal carcinoma cell lines with various metastatic potentialities].[具有不同转移潜能的鼻咽癌细胞系中的差异表达基因]
Zhonghua Zhong Liu Za Zhi. 2002 Sep;24(5):430-4.
8
[Differentially expressed genes between upward and downward progressing types of nasopharyngeal carcinoma].[鼻咽癌向上和向下进展类型之间的差异表达基因]
Ai Zheng. 2008 May;27(5):460-5.
9
Microarray analysis of differentially expressed genes between nasopharyngeal carcinoma cell lines 5-8F and 6-10B.鼻咽癌5-8F和6-10B细胞系之间差异表达基因的微阵列分析。
Cancer Genet Cytogenet. 2010 Jan 1;196(1):23-30. doi: 10.1016/j.cancergencyto.2009.08.004.
10
[Identification of down-regulated expressed sequence tag at chromosome 3p21 in nasopharyngeal carcinoma].[鼻咽癌中3号染色体短臂21区下调表达序列标签的鉴定]
Ai Zheng. 2003 Jan;22(1):1-5.

引用本文的文献

1
MicroRNA-663 facilitates the growth, migration and invasion of ovarian cancer cell by inhibiting TUSC2.MicroRNA-663 通过抑制 TUSC2 促进卵巢癌细胞的生长、迁移和侵袭。
Biol Res. 2019 Apr 3;52(1):18. doi: 10.1186/s40659-019-0219-6.
2
miR-663b promotes tumor cell proliferation, migration and invasion in nasopharyngeal carcinoma through targeting TUSC2.微小RNA-663b通过靶向TUSC2促进鼻咽癌肿瘤细胞的增殖、迁移和侵袭。
Exp Ther Med. 2017 Aug;14(2):1095-1103. doi: 10.3892/etm.2017.4608. Epub 2017 Jun 14.
3
Analysis of Argonaute Complex Bound mRNAs in DU145 Prostate Carcinoma Cells Reveals New miRNA Target Genes.
DU145前列腺癌细胞中与AGO蛋白复合体结合的mRNA分析揭示了新的miRNA靶基因。
Prostate Cancer. 2017;2017:4893921. doi: 10.1155/2017/4893921. Epub 2017 Jan 5.
4
Identification of guanine nucleotide-binding protein γ-7 as an epigenetically silenced gene in head and neck cancer by gene expression profiling.通过基因表达谱分析鉴定头颈部癌中鸟嘌呤核苷酸结合蛋白 γ-7 为表观遗传沉默基因。
Int J Oncol. 2013 Apr;42(4):1427-36. doi: 10.3892/ijo.2013.1808. Epub 2013 Feb 6.
5
Targeted gene therapy of nasopharyngeal cancer in vitro and in vivo by enhanced thymidine kinase expression driven by human TERT promoter and CMV enhancer.人端粒酶逆转录酶启动子和 CMV 增强子驱动的增强型胸苷激酶表达对鼻咽癌细胞的体内外靶向基因治疗。
J Exp Clin Cancer Res. 2010 Jul 13;29(1):94. doi: 10.1186/1756-9966-29-94.